A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625087



Internal ID21573392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44746201..44746201hg38UCSC Ensembl
chr7:44785800..44785800hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150499
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625087
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer